Variant #0000557856 (NC_000016.9:g.30199762T>C, NM_007074.3:c.1146T>C (CORO1A))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.30199762T>C
DNA change (hg38) g.30188441T>C
Published as CORO1A(NM_007074.3):c.1146T>C (p.G382=), CORO1A(NM_007074.4):c.1146T>C (p.G382=)
ISCN -
DB-ID BOLA2B_000001 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00254 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLX1A NM_001014999.2 -?/. - c.-5644T>C r.(?) p.(=)
BOLA2B NM_001039182.1 -?/. - c.*4534A>G r.(=) p.(=)
CORO1A NM_007074.3 -?/. - c.1146T>C r.(?) p.(Gly382=)


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